Product Details
- SNP ID
-
rs145815177
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:63638070 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTAACCTGCTGAAGTTTTGCCAGAA[A/T]GGTGACTGGCTGCGCTTGGGTTCGG
- Phenotype
-
MIM: 300429
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ARHGEF9
PubMed Links
Gene Details
- Gene
- ARHGEF9
- Gene Name
- Cdc42 guanine nucleotide exchange factor 9
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001173479.1 |
2437 |
Silent Mutation |
CCA,CCT |
P450P |
NP_001166950.1 |
| NM_001173480.1 |
2437 |
Silent Mutation |
CCA,CCT |
P401P |
NP_001166951.1 |
| NM_015185.2 |
2437 |
Silent Mutation |
CCA,CCT |
P503P |
NP_056000.1 |
| XM_005262249.2 |
2437 |
Silent Mutation |
CCA,CCT |
P510P |
XP_005262306.1 |
| XM_005262250.3 |
2437 |
Silent Mutation |
CCA,CCT |
P482P |
XP_005262307.1 |
| XM_005262251.1 |
2437 |
Silent Mutation |
CCA,CCT |
P482P |
XP_005262308.1 |
| XM_005262252.1 |
2437 |
Silent Mutation |
CCA,CCT |
P482P |
XP_005262309.1 |
| XM_011530890.1 |
2437 |
Silent Mutation |
CCA,CCT |
P503P |
XP_011529192.1 |
| XM_011530892.1 |
2437 |
Silent Mutation |
CCA,CCT |
P443P |
XP_011529194.1 |
| XM_017029363.1 |
2437 |
Silent Mutation |
CCA,CCT |
P508P |
XP_016884852.1 |
| XM_017029364.1 |
2437 |
Silent Mutation |
CCA,CCT |
P508P |
XP_016884853.1 |
| XM_017029365.1 |
2437 |
Silent Mutation |
CCA,CCT |
P503P |
XP_016884854.1 |
| XM_017029366.1 |
2437 |
Silent Mutation |
CCA,CCT |
P503P |
XP_016884855.1 |
| XM_017029367.1 |
2437 |
Silent Mutation |
CCA,CCT |
P482P |
XP_016884856.1 |
| XM_017029368.1 |
2437 |
Silent Mutation |
CCA,CCT |
P482P |
XP_016884857.1 |
| XM_017029369.1 |
2437 |
Silent Mutation |
CCA,CCT |
P466P |
XP_016884858.1 |
| XM_017029370.1 |
2437 |
Silent Mutation |
CCA,CCT |
P459P |
XP_016884859.1 |
| XM_017029371.1 |
2437 |
Silent Mutation |
CCA,CCT |
P438P |
XP_016884860.1 |
| XM_017029372.1 |
2437 |
Silent Mutation |
CCA,CCT |
P438P |
XP_016884861.1 |
| XM_017029373.1 |
2437 |
Silent Mutation |
CCA,CCT |
P401P |
XP_016884862.1 |
| XM_017029374.1 |
2437 |
Silent Mutation |
CCA,CCT |
P399P |
XP_016884863.1 |
| XM_017029375.1 |
2437 |
UTR 3 |
|
|
XP_016884864.1 |
| XM_017029376.1 |
2437 |
Intron |
|
|
XP_016884865.1 |
| XM_017029377.1 |
2437 |
UTR 3 |
|
|
XP_016884866.1 |
| XM_017029378.1 |
2437 |
Intron |
|
|
XP_016884867.1 |
| XM_017029379.1 |
2437 |
UTR 3 |
|
|
XP_016884868.1 |
| XM_017029380.1 |
2437 |
UTR 3 |
|
|
XP_016884869.1 |
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